A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894197



Internal ID19185266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:61632502..61655297hg38UCSC Ensembl
Outerchr5:61632502..61661308hg38UCSC Ensembl
Innerchr5:60928329..60951124hg19UCSC Ensembl
Outerchr5:60928329..60957135hg19UCSC Ensembl
Innerchr5:60964086..60986881hg18UCSC Ensembl
Outerchr5:60964086..60992892hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3828807
hg1928807
hg1828807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799882, essv25779060, essv25781755, essv25799667, essv25783796
Samples
Known GenesC5orf64
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894197
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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